Patent Grant
11897923
This invention generally relates to the technical field of plant genetic engineering, and more particularly, to a coding gene of the SOSEKI protein SOK2 relating to plants' unknown functions and an application thereof in increasing the plant biomass and fermentable sugar yield.
As the global population explodes, the consumption of fossil energy has soared, which urgently demands development of renewable energies. Biomass energy has become the most promising alternative energy resource for being rich, eco-friendly, clean and renewable. Presently, the research and development of biomass energy are primarily focused on biodiesel and bioethanol, wherein the use of bioethanol has been gradually commercialized. Lignocellulose, a general name for cellulose, hemicellulose and lignin, is the most plentiful and eco-friendly bioethanol raw material in the world. Panicum virgatum, which is a tall perennial C4 herbaceous plant, is an important fiber biomass resource used mainly as an energy or forage grass. It grows rapidly, possesses high biomass, is widely adaptable, has strong stress resistance, and is capable of growing on saline-alkali, arid and barren lands. Therefore, increasing the biomass and fermentable sugar yield of Panicum virgatum to significantly improve the development and use of its biomass energy is of high practical value. The completion of the entire genome sequencing of Panicum virgatum, the creation of gene expression database and the improvement of transformation system effectively ensure the resource for the discovery and identification of functional genes.
SOSEKI (SOK) proteins are proteins which contain DIX-like domains and are extremely conservative in animal and plant evolutions. The functions of SOSEKI (SOK) protein family have not been deeply studied yet. In addition to participating in the cell polar development, studies show that AtSOK2 may also regulate the flowering time of arabidopsis after vernalization. AtSOK2 is located 4.7 kb upstream of the same chromosome of the flowering time negative regulation factor FLC, and thus it is also called UPSTREAM OF FLC (UFC: At5g10150). Resembling the FLC, the expression level of the SOK2 is significantly lowered after the vernalization. The expression variations of the FLC and the SOK2 are consistent in different non-vernalized ecotype arabidopsis plants. For instance, the transcriptional levels of the FLC and the SOK2 in the late flowering ecotype plants are higher than in early flowering ecotype plants. Moreover, these genes show resembling developmental regulation expression patterns: the transcriptional level descends in germinating seeds, but ascends significantly before the first pair of leaves appear. Similarly, in late flowering arabidopsis mutants, the FLC and the SOK2 coordinate to regulate the flowering time according to different gene locus modifications (Finnegan et al, A Cluster of Arabidopsis Genes with a Coordinate Response to an Environmental Stimulus. Current Biology, 14: 911-916). Presently, the studies on the function of the SOK gene and its protein in other plants are scanty.
The purpose of the present invention is to provide a coding gene of the plant SOSEKI protein SOK2 and an application thereof in increasing the plant biomass and fermentable sugar yield. According to the present invention, the technical problems relating to the low biomass energy of plants, insufficient resource of modified genes, as well as the failure of simultaneously meeting the needs of increasing the plant yield and improving the cell wall molecular quality are effectively solved.
To achieve the above purposes, the present invention adopts the following technical solution:
The first purpose of the present is to provide a coding gene of the Panicum virgatum SOSEKI protein SOK2, wherein its amino acid sequence is shown in SEQ ID No.2.
The present invention also provides a coding gene of the Panicum virgatum SOSEKI protein SOK2, wherein its nucleotide sequence is shown in SEQ ID No.1.
The second purpose of the present invention is to provide a recombinant vector pANIC6B-PvSOK2 containing the gene of the Panicum virgatum SOSEKI protein SOK2.
The third purpose of the present invention is to provide a method for improving the expression level of the SOSEKI protein SOK2 in plants, which utilizes the overexpression vector in the second purpose to improve the expression level of the SOK2 in Panicum virgatum.
The fourth purpose of the present invention is to provide an application of the Panicum virgatum SOSEKI protein SOK2 in regulating the flowering time of plants.
The fifth purpose of the present invention is to provide an application of the Panicum virgatum SOSEKI protein SOK2 in increasing the plant biomass and fermentable sugar yield.
To obtain the gene sequence of the SOSEKI protein SOK2 in the CDS region, primers PvSOK2-F and PvSOK2-R are designed on both sides of the PvSOK2 full-length gene sequence according to the Panicum virgatum genome information published on the Phytozome website. A 732 bp full-length gene sequence of the SOSEKI protein PvSOK2 is obtained by means of PCR (Polymerase Chain Reaction) amplification. Subsequently, the full-length sequence fragment is recombined and integrated into the overexpression vector pANIC6B based on the Gateway technology. Through adopting the genetic transformation method mediated by the agrobacterium EHA105, the gene is transformed into the embryogenic calli of Panicum virgatum, thereby obtaining resistant regenerated plants through the hygromycin resistance screening. Finally, the positive transgenic plants are identified by PCR analysis. The test results show that the overexpressing SOK2 effectively delays the flowering time, increases the plant biomass and boosts the fermentable sugar yield.
The core features and the inventive concept of the present invention are the following:
Compared with the prior art, the present invention has the following advantages:
Detailed embodiments and drawings are combined hereinafter to further elaborate the technical solution of the present invention.
The materials, reagents and molecular marker probes adopted in the following embodiments may be purchased from the market unless stated otherwise.
According to the published genome information of Panicum virgatum in the Phytozome website, primers PvSOK2-F and PvSOK2-R are designed on both sides of the PvSOK2 full-length sequence. Taking the Panicum virgatum cDNA as a template, the PCR amplification is performed with the aforesaid primers.
The primers' sequences are as follows:
The PCR reaction system is: 2 μL of cDNA, 25 μL of 2×Buffer, 4 μL of 10 pM dNTP, 2 μL of 10 μM forward/reverse primer (respectively), 0.5 μL of 5 U/μL PrimerSTAR HS DNA polymerase and 14.5 μL of ddH2O. The sample is added on the ice and then mixed uniformly. The PCR reaction conditions are: 98° C. for 3 minutes; 98° C. for 5 seconds, 56° C. for 15 seconds; 72° C. for 30 seconds, 35 cycles, and 72° C. for 5 minutes. The PCR amplified product is detected by using 1% agarose gel electrophoresis, and then the fragment having a size of about 750 bp are obtained (shown in
Taking the aforesaid sequence fragment as a template, the PvSOK2 is designed with a primer capable of being seamlessly joined with the expression vector pCABIA1300-cGFP, and the fragment is amplified by using a high-fidelity enzyme. The expression vector is digested by the HindIII restriction enzyme. After the PvSOK2 gene fragment and the pCABIA1300-cGFP vector fragment are extracted, a joining enzyme (purchased from Vazyme company) is adopted to join the two fragments through homologous recombination. The joined product is transformed into Escherichia coli DH5a competent cells by heat shock. Monoclonal bacterial colonies are selected and cultured in the liquid LB medium containing kanamycin for PCR amplification and sequencing identification, thereby obtaining the recombinant plasmid pCABIA1300-PvSOK2-cGFP.
The constructed recombinant vector pCABIA1300-PvSOK2-cGFP is transformed into the agrobacterium EHA105 and the strain is preserved. The bacterial solution is injected into tobacco by means of the transient expression technology to observe the subcellular localization. The fluorescence confocal results show that, different from typical transcription factors, the PvSOK2 can be localized in not only the tobacco cell nucleus but also the cell membrane, meaning that the gene may have other important biological functions other than functioning as a transcription factor.
The primers PvSOK2-pGWC-F and PvSOK2-pGWC-R for joining an entry vector are designed in the overexpression vector. 18 bases (seamless joining sequence) after the AhdI restriction site and the entry vector pGWC restriction site are introduced at the end of the primers. Taking the obtained PvSOK2 full-length sequence as a template, the PCR amplification is performed with the aforesaid primers.
The primers' sequences are as follows:
wherein the underlined portions are the seamless joining sequences.
The amplified fragments are extracted. The pGWC vector is digested with the AhdI restriction enzyme and is then extracted. A joining enzyme (purchased from Vazyme company) is adopted to join the two fragments through homologous recombination. The joined product is transformed into Escherichia coli DH5a competent cells by heat shock. Monoclonal colonies are selected and cultured in the liquid LB medium containing kanamycin for sequencing identification. The recombinant strain plasmid is extracted and sequenced correctly by using the reagent kit, and the recombinant plasmid extracted fragments are integrated into the overexpression vector pANIC6B using the Gateway technology (shown in
In the method (Xi et al, Agrobacterium-mediated transformation of switchgrass and inheritance of the transgenes. 2009, Bioenergy Research, 2: 275-283), the pANIC6B-PvSOK2 is introduced into the lowland wild Panicum virgatum Alamo to obtain resistant seedlings, the vector universal primer ZmUbq-F and the downstream primer PvSOK2-R of the target gene are used to detect the target gene, and upstream and downstream primers (hph3+hph4) of the hygromycin-resistant gene are used to detect the hygromycin gene, thus finally determining the positive transgenic lines (shown in
The tender stem tissues of the aforesaid identified transgenic plants are taken and the total RNA is extracted by using a TriZol® (guanidinium thiocyanate) reagent kit (Invitrogen, product No.: 15596026). The content and purity of the total RNA are detected by using an agarose gel electrophoresis and nucleic acid analyzer (NanoDrop® (microvolume spectrophotometer)). Subsequently, 1.0 μg of total RNA is taken for reverse transcription, and a reverse transcriptase (Promega, product No.: M1701) is adopted to reverse-transcriptase it into cDNA, wherein the reverse transcriptional reaction process is referred to the Instructions. Taking the aforesaid cDNA as a template, the primers PvSOK2-qRT-F and PvSOK2-qRT-R are used for fluorescent quantitative PCR detection, and the reference gene is the Ubiquitin (UBQ) gene of Panicum virgatum. The sequences of the primers are as follows:
The real-time fluorescent quantitative PCR reaction system is 20 μL, including 1 μL of forward/reverse primer (respectively), 2 μL of cDNA template, 10 μL of SYBR Green qRT Master Mix (purchased from Takara Bio Inc.) and ddH2O (supplements to 20 μL). The model no. of the real-time fluorescent quantitative PCR is Roche480 and a two-step method is adopted to perform the reaction. The test results show that, compared with the wild Control, the expression levels of the PvSOK2 in the transgenic plants PvSOK2_OE-14, PvSOK2_OE-35 and PvSOK2_OE-36 are significantly increased (shown in
The flowering time and biomass of the transgenic plants growing for 6 months are measured. Compared with the control plant, the flowering time of transgenic plants is delayed (shown in
The general principle defined in the specification may be realized in other embodiments without departing from the spirit or scope of the present invention. Therefore, the present invention is not limited to the aforesaid embodiments but to the widest scope consistent with the principles and inventive features disclosed in the present invention.
| Number | Date | Country | |
|---|---|---|---|
| 20220153785 A1 | May 2022 | US |
